Alkylation of 5-phenyltetrazole with isopropyl alcohol in 84-99% sulfuric acid medium occurs regioselectively a t N2 position of the heterocycle to produce 2-isopropyl-5-phenyltetrazole. The regioselectivity is conditioned by lH, 4H-5-phenyltetrazolium cation being the alkylation substratum. The rea
Kinetics and mechanisms of substitution reactions with sulfur-containing nucleophiles in aqueous acid solutions. I—rates of reactions of some tetrahalopalladate (II) anions with thiourea and selenourea
✍ Scribed by P. Van Z. Bekker; W. Robb
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 545 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
The activation energy parameters for the reaction of PdX (X=Cl^−^, Br^−^) in aqueous halide acid solution with thiourea (tu) and selenourea (seu) have been determined. High rates of reaction parallel low enthalpies and appreciable negative entropy of activation. The rate law in each case simplifies to k~obs~=k[L] where L=tu or seu, and only ligand‐dependent rate constants are observed at 25°C. The ligand‐dependent rate constants for the first identifiable step in the PdCl + X system is (9.1±0.1) × 10^3^ M^−1^ sec^−1^ and (4.5±0.1) × 10^4^ M^−1^ sec^−1^ for X=tu and seu, respectively, while for the PdBr + X system it is (2.0±0.1) × 10^4^ M^−1^ sec^−1^ and (9.0±0.1) × 10^4^ M^−1^ sec^−1^ for X=tu and seu, respectively.
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